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采用反相高效液相色谱法对倍他米松或地塞米松活性药物成分中的痕量倍他米松或地塞米松进行定量分析。

Quantitation of trace betamethasone or dexamethasone in dexamethasone or betamethasone active pharmaceutical ingredients by reversed-phase high-performance liquid chromatography.

作者信息

Xiao Kang Ping, Xiong Yuan, Rustum Abu M

机构信息

Global Quality Services-Analytical Sciences, Schering-Plough Corporation, 1011 Morris Avenue, Union, NJ 07083, USA.

出版信息

J Chromatogr Sci. 2008 Jan;46(1):15-22. doi: 10.1093/chromsci/46.1.15.

Abstract

Adequate separation is essential for the quantitation of trace amounts of dexamethasone that are typically found in betamethasone active pharmaceutical ingredients and vice versa. In this paper, we describe three simple and efficient high-performance liquid chromatography methods from which true baseline separations between betamethasone and dexamethasone are achieved even when the concentration ratios between these two epimers are larger than 2000:1. One method is developed on a 5 cm ACE C8 column that uses water and acetonitrile as the mobile phase and 20 mM beta-cyclodextrin as the mobile phase additive. The resolution factor between betamethasone and dexamethasone is 3.3. The second method is developed on a 10 cm ACE C8 column that uses water and acetonitrile as the mobile phase, in which the resolution factor between the epimers is 2.7. The third method is developed on a 10 cm ACE C8 column using water and tetrahydrofuran as the mobile phase, in which the resolution factor between the epimers is 3.1. Preliminary validation studies are carried out for the second and third methods.

摘要

对于定量测定倍他米松活性药物成分中通常含有的痕量地塞米松,以及反之对于定量测定地塞米松活性药物成分中通常含有的痕量倍他米松而言,充分分离至关重要。在本文中,我们描述了三种简单高效的高效液相色谱方法,即使这两种差向异构体之间的浓度比大于2000:1,也能实现倍他米松和地塞米松之间真正的基线分离。一种方法是在5 cm的ACE C8柱上开发的,该方法使用水和乙腈作为流动相,并使用20 mM的β-环糊精作为流动相添加剂。倍他米松和地塞米松之间的分离度因子为3.3。第二种方法是在10 cm的ACE C8柱上开发的,该方法使用水和乙腈作为流动相,其中差向异构体之间的分离度因子为2.7。第三种方法是在10 cm的ACE C8柱上开发的,使用水和四氢呋喃作为流动相,其中差向异构体之间的分离度因子为3.1。对第二种和第三种方法进行了初步验证研究。

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